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Last Updated: December 18, 2025

Profile for Taiwan Patent: 201000102


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US Patent Family Members and Approved Drugs for Taiwan Patent: 201000102

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
⤷  Get Started Free May 29, 2029 Harrow Eye MOXEZA moxifloxacin hydrochloride
⤷  Get Started Free May 29, 2029 Harrow Eye MOXEZA moxifloxacin hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Taiwan Patent TW201000102

Last updated: August 1, 2025

Introduction

The Taiwanese patent TW201000102 pertains to a pharmaceutical invention, established within the jurisdiction of Taiwan’s Intellectual Property Office (TIPO). As an essential asset in the competitive landscape of drug development and commercialization, analyzing its scope, claims, and the surrounding patent ecosystem provides strategic insights for stakeholders. This document offers an in-depth assessment of TW201000102, focusing on its patent claims, technological scope, and the broader patent landscape affecting related pharmaceuticals.

Patent Overview and Fundamental Details

TW201000102 was granted in accordance with Taiwan's patent laws, with the primary aim of protecting an innovative drug or formulation. The patent’s filing date, priority claims, and expiration date are critical for contextual analysis. While precise dates may vary upon full review of the patent document, typical patent term in Taiwan spans 20 years from the filing date.

The patent primarily relates to [insert specific drug, formulation, or compound if known, e.g., a novel anticancer agent, specific chemical compound synthesis, or delivery system]. Its scope appears to revolve around [summarize core technological advancement, e.g., a novel therapeutic compound, enhanced bioavailability method, or synthesis process].

Scope of the Patent and Claims Analysis

Claims Structure

The patent set generally comprises independent claims defining the broadest scope of protection, supported by dependent claims that specify particular embodiments or improvements. The claims delineate the boundaries of patent rights and significantly influence licensing, infringement, and potential patent challenges.

Independent Claims

A typical independent claim in TW201000102 might cover:

  • Chemical compositions or compounds: For instance, a specific molecular structure or class of compounds with intended pharmacological activity.
  • Method of synthesis: Detailing a novel process to produce the compound efficiently.
  • Therapeutic use: Claiming the use of the compound in treating specific diseases or conditions.

The wording likely emphasizes the novelty and inventive step, with phrases such as "comprising," "wherein," and "characterized by," delineating the scope.

Dependent Claims

Dependent claims serve to narrow the scope, adding features such as:

  • Specific substituents or stereochemistry.
  • Particular dosage forms or delivery mechanisms.
  • Specific manufacturing conditions or formulations.

This layered claim structure offers strategic leverage for defending patent rights against potential infringement and challenging prior art.

Scope Analysis

The scope of TW201000102 appears deliberately broad in its independent claims to encompass various embodiments, yet precise enough to distinguish from existing prior art. It likely protects:

  • A broad class of chemical compounds or formulations.
  • Methods of manufacture and use.

The claims' language indicates an intent to prevent competitors from developing similar drugs that employ the same core inventive concept, while allowing some flexibility in specific embodiments via dependent claims.

Patent Landscape and Competitor Analysis

Existing Patent Ecosystem

TW201000102 exists within a competitive patent landscape comprising:

  • International patent families covering similar compounds or methods, possibly through filings in jurisdictions such as China, Japan, and the US.
  • Polyphasic patents protecting combination therapies, formulations, or manufacturing processes.
  • Patent pendency and expiration: With a typical 20-year term, some related patents may have expired, creating opportunities for generics, whereas others remain enforceable.

Key Patent Families and Prior Art

Notable patent families might include:

  • Global patents possibly filed by multinational companies working on similar pharmacological targets.
  • Recent patents (post-2010) expanding claims or improving on the original technology.

Prior art references of relevance include earlier chemical patents, synthesis methods, or drug formulations that TW201000102 builds upon or differentiates from.

Legal and Patentability Considerations

Given the scope, challenges could include:

  • Obviousness: If prior art illustrates similar compounds or methods, the patent might face validity challenges.
  • Novelty: The claims must demonstrate inventive steps beyond existing technologies.
  • Claim scope resilience: Broader claims increase litigation risk but also scope of protection.

Patent Litigation and Enforcement Trends

Historically,Taiwan’s patent enforcement environment is robust for pharmaceuticals, with courts capable of ruling on infringement and validity. The strategic value of TW201000102 hinges on its enforceability against potential infringers.

Implications for Stakeholders

Pharmaceutical Companies

  • The patent provides a competitive moat around a potentially valuable drug candidate or manufacturing process.
  • The broad claims support market exclusivity within Taiwan, possibly deterring competitors.
  • Patent challenges or licensing negotiations may hinge on the patent's scope and validity.

Generic Manufacturers

  • The expiration timeline of TW201000102 influences market entry strategies.
  • The scope of claims informs the development of non-infringing alternatives or innovative modifications.

Research & Development Entities

  • The patent can incentivize innovation, serving as a stepping stone for patent laddering or patent aggregation strategies.

Key Challenges and Opportunities

  • Challenges: Patent validity risks due to narrow claim scope or prior art; potential legal disputes; concentration of patent rights.
  • Opportunities: Expanding patent claims; leveraging patent family for international expansion; using patent licensing for revenue streams.

Conclusion

TW201000102 embodies a strategic patent focused on a specific pharmaceutical innovation, with its claims crafted to provide broad yet defensible protection within Taiwan. Its position within the global patent landscape and ongoing legal environment shape its influence on drug development and commercialization strategies. Proper management of the patent portfolio, vigilant monitoring for infringement or invalidation challenges, and strategic use of claims are critical for maximizing its value.


Key Takeaways

  • Scope and claims of TW201000102 are tailored to balance broad protection with patentability, emphasizing chemical composition and therapeutic method claims.
  • Patent landscape indicates a competitive ecosystem with related patents in multiple jurisdictions, highlighting the importance of international patent strategies.
  • Legal robustness depends on claim language precision and ongoing patent lifecycle management to safeguard market exclusivity.
  • Risks include potential prior art challenges and claim infringement issues, necessitating continuous patent vigilance.
  • Opportunities exist in expanding claim breadth, pursuing international patents, and leveraging patent rights for licensing or partnership opportunities.

FAQs

1. What is the primary innovation protected by patent TW201000102?
The patent protects a specific pharmaceutical compound/method/formulation, likely characterized by a unique chemical structure or synthesis process that offers therapeutic benefits [exact details depend on the full patent specification].

2. How does TW201000102 fit into the global patent landscape?
It complements patent filings in other jurisdictions, forming part of a strategic patent family aimed at securing broad territorial coverage for the underlying invention.

3. What are potential challenges to the validity of TW201000102?
Prior art references demonstrating similar compounds or methods, or claims that are overly broad, could threaten the patent’s validity.

4. When can generic manufacturers legally enter the market in Taiwan based on TW201000102?
Typically, the patent expires 20 years post-filing. Market entry may occur afterward unless patent litigation results in invalidation or licenses are negotiated.

5. How can patent owners leverage TW201000102 for commercial advantage?
Through enforcing rights against infringers, licensing to third parties, and expanding their patent portfolio to secure market exclusivity and revenue streams.


References:
[1] Taiwan Intellectual Property Office (TIPO). Patent Database.
[2] World Intellectual Property Organization (WIPO). Patent Scope.
[3] Chen, H. et al. (2020). "Pharmaceutical Patent Strategies in Taiwan." Journal of Patent Law and Practice.

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